Abstract
Celling chemistry: Ketones (secondary alcohols) can be biocatalytically reduced (oxidized) at a substrate concentration of up to 1.8 mol L-1 in an asymmetric fashion by employing a novel secondary alcohol dehydrogenase from Rhodococcus ruber DSM 44541 (see scheme). Furthermore, the enzyme is exceptionally stable at high cosubstrate concentrations, that is, 2-propanol (50% v/v) for reduction and acetone (20% v/v) for oxidation, respectively.
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Stampfer, W., Kosjek, B., Moitzi, C., Kroutil, W., & Faber, K. (2002). Biocatalytic asymmetric hydrogen transfer. Angewandte Chemie - International Edition, 41(6), 1014–1017. https://doi.org/10.1002/1521-3773(20020315)41:6<1014::AID-ANIE1014>3.0.CO;2-6
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